N-(2-fluropropyl)-4-methyl-N-(4-trifluoromethylphenyl)benzenesulfonamide

Base Information

Chemical Name:N-(2-fluropropyl)-4-methyl-N-(4-trifluoromethylphenyl)benzenesulfonamide
CAS No.:1443775-66-3
Molecular Formula:C₁₇H₁₇F₄NO₂S
Molecular Weight:375.387
Hs Code.:

Synonyms:N-(2-fluropropyl)-4-methyl-N-(4-trifluoromethylphenyl)benzenesulfonamide

Suppliers and Price of N-(2-fluropropyl)-4-methyl-N-(4-trifluoromethylphenyl)benzenesulfonamide

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
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price

Total 2 raw suppliers

Chemical Property of N-(2-fluropropyl)-4-methyl-N-(4-trifluoromethylphenyl)benzenesulfonamide

Chemical Property:

Purity/Quality:: 98% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of N-(2-fluropropyl)-4-methyl-N-(4-trifluoromethylphenyl)benzenesulfonamide

There total 4 articles about N-(2-fluropropyl)-4-methyl-N-(4-trifluoromethylphenyl)benzenesulfonamide which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 97.0%

: 1443775-44-7
N-allyl-4-methyl-N-[4-(trifluoromethyl)phenyl]benzenesulfonamide

: 1443775-66-3
N-(2-fluropropyl)-4-methyl-N-(4-trifluoromethylphenyl)benzenesulfonamide

Guidance literature:: With hydrogen fluoride; antimony pentafluoride; at -65 ℃; for 0.166667h;
DOI:10.1039/c3cc40858b

Reference yield:

: 107491-54-3
4-methyl-N-(4-trifluoromethyl-phenyl)-benzenesulfonamide

: 1443775-66-3
N-(2-fluropropyl)-4-methyl-N-(4-trifluoromethylphenyl)benzenesulfonamide

Guidance literature:: Multi-step reaction with 2 steps

1: potassium carbonate / dichloromethane / 16 h / 80 °C / Inert atmosphere

2: hydrogen fluoride; antimony pentafluoride / 0.17 h / -65 °C

With hydrogen fluoride; antimony pentafluoride; potassium carbonate; In dichloromethane;
DOI:10.1039/c3cc40858b

Reference yield:

: 98-59-9
p-toluenesulfonyl chloride

: 1443775-66-3
N-(2-fluropropyl)-4-methyl-N-(4-trifluoromethylphenyl)benzenesulfonamide

Guidance literature:: Multi-step reaction with 3 steps

1: pyridine / dichloromethane / 48 h / 0 - 20 °C / Inert atmosphere

2: potassium carbonate / dichloromethane / 16 h / 80 °C / Inert atmosphere

3: hydrogen fluoride; antimony pentafluoride / 0.17 h / -65 °C

With pyridine; hydrogen fluoride; antimony pentafluoride; potassium carbonate; In dichloromethane;
DOI:10.1039/c3cc40858b